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Turkish Republic
Ministry of Higher Education and Scientific Research
University of Cukurova
Biotechnology and science
BLUEBERRIES MICROPROPAGATION
Awara M. HAMAKHAN
PhD. Student from plant tissue culture
Email: Awarahamakhan@yahoo.com
2021
Kurdistan Regional Government
Ministry of Higher Education and Scientific Research
Sulaimani Polytechnic University
Bakrajo Technical Agriculture Institute
General information of blueberry
 The genus Vaccinium, a member of the
family Ericaceae, has approximately 400
species distributed to all continents
 The blueberry bush is a flowering shrub 4
m for highbush
 Blueberries fruit are small 5–16
millimeters in diameter and feature a
flared crown at the end with purple color.
Fruit nutrient
 Blueberries are among the most nutrient are
low in calories but high in nutrients
From 1-cup (148-gram) serving of blueberries
contains :
 Fiber: 4 grams
 Vitamin C: 24%
 Vitamin K: 36%
 Manganese: 25%
 Water : 85%
 Calories :84
 Carbohydrates: 15 grams
Medicinal used
 Inside the fruit have anthocyanin flavonoid that
often powerful antioxidant effect they have been
shown to protect against heart disease and cancer
, and can also help maintain bone strength,
mental health, and healthful blood pressure.
 Plant foods may also promote hair and skin
health, increased energy, and overall lower
weight.
Plant propagation
Two different methods for propagation
 Generative (sexual) Propagation
 Vegetative (asexual) Propagation:
Softwood and hardwood cuttings
Traditional propagation methods are
also not particularly efficient as regards
the number
 in vitro propagation
Plant propagation
 in vitro propagation of blueberries take explant through
axillary leaf bud branching.
Plant sterilization
 Filed treatment: The best way for controlled
fungus from explant must be apply fungicide
before take the explant from the filed.
 For more controlled disease, better to apply
pesticide or fungicide by irrigation to mother
plant.
Plant surface sterilization
 Wash the brunch by tap water to remove the soil
 Cut them into smaller pieces 1-3 cm with single node
explants .
 Surface sterilization; with anti bacterial and fungicide
0.1 % for 10 minute.
 sodium hypochlorite 20 % and add Tween-20 (1%)
shake for 10 min.
 Wash the pieces several times with sterile water
 In some cases should be change sodium
hypochlorite concentration and time
 If the explants is not clean should be use 0.1%
solution of mercuric chloride for 2-5 min.
Medium used
 As a basal culture medium
Anderson’s Rhododendron
medium - AN (Anderson,1980)
is efficiently used for shoot
initiation
 Alternatively for shoot
induction and multiplication
modified WPM (McCown
Woody Plant Medium) (Lloyd
and McCown,1980)
 20 g/L sucrose, 6 g/L agar
Hormones
 Cytokinin group hormone commonly zeatin riboside
apply to Initiation and multiplication shoots in blueberry
 Zeatin 1.0 mg/L show high number shoot multiplication.
 2ip-isopen-tenyladenine 2.0 mg/l, is the alternative
hormone for shoot multiplication
 TDZ- Thidiazuron, 1.0 mg/L is second alternative
cytokinin for shoot multiplication.
 IBA- Indole-3-butyric acid 0.1- 1.0 mg/L, is auxins group
supported callus and root formation
 GA3- Gibberellic acid 0.1-0.5 mg/L, have supported plant
length
pH for the blueberry media
 In highbush blueberry
micropropagation, shoot growth or
plantlet development is also highly
sensitive to other environmental
conditions, including pH,
temperature, sucrose, humidity and
growing substrate
 pH is adjusted 5.1-5.5 for shoot
multiplication
 Root formation and shoot thickness
pH is 4.5-5.0.
Root formation
The best media for rooting :
 Anderson medium or WPM
supplemented with 0.8-1.0 mg/L IBA
and 1.0 g/L activated charcoal and the
pH adjusted 4.5
 Sucrose 15 mg/L
 Agar 6.5-7.0 g/L
Acclimatization process
 Primary hardening in mist chamber culture plants on peat substrate with green
leaves and roots were first kept in the mist chamber for 14 days.
 Graded plant were transferred nursery and spray NPK 19:19:19 5g/15 litter
water with fungicide and regular irrigation and gradually lowering the
humidity by ventilation for 2-4 weeks
 Secondary hardening plantlets in height 8-10 cm (after 2 months) were
replanted into bigger containers (12.0 cm in diameter) and transferred to open-
air conditions.
Tanks for listening

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berries presentation Awara.pptx

  • 1. Turkish Republic Ministry of Higher Education and Scientific Research University of Cukurova Biotechnology and science BLUEBERRIES MICROPROPAGATION Awara M. HAMAKHAN PhD. Student from plant tissue culture Email: Awarahamakhan@yahoo.com 2021 Kurdistan Regional Government Ministry of Higher Education and Scientific Research Sulaimani Polytechnic University Bakrajo Technical Agriculture Institute
  • 2. General information of blueberry  The genus Vaccinium, a member of the family Ericaceae, has approximately 400 species distributed to all continents  The blueberry bush is a flowering shrub 4 m for highbush  Blueberries fruit are small 5–16 millimeters in diameter and feature a flared crown at the end with purple color.
  • 3. Fruit nutrient  Blueberries are among the most nutrient are low in calories but high in nutrients From 1-cup (148-gram) serving of blueberries contains :  Fiber: 4 grams  Vitamin C: 24%  Vitamin K: 36%  Manganese: 25%  Water : 85%  Calories :84  Carbohydrates: 15 grams
  • 4. Medicinal used  Inside the fruit have anthocyanin flavonoid that often powerful antioxidant effect they have been shown to protect against heart disease and cancer , and can also help maintain bone strength, mental health, and healthful blood pressure.  Plant foods may also promote hair and skin health, increased energy, and overall lower weight.
  • 5. Plant propagation Two different methods for propagation  Generative (sexual) Propagation  Vegetative (asexual) Propagation: Softwood and hardwood cuttings Traditional propagation methods are also not particularly efficient as regards the number  in vitro propagation
  • 6. Plant propagation  in vitro propagation of blueberries take explant through axillary leaf bud branching.
  • 7. Plant sterilization  Filed treatment: The best way for controlled fungus from explant must be apply fungicide before take the explant from the filed.  For more controlled disease, better to apply pesticide or fungicide by irrigation to mother plant.
  • 8. Plant surface sterilization  Wash the brunch by tap water to remove the soil  Cut them into smaller pieces 1-3 cm with single node explants .  Surface sterilization; with anti bacterial and fungicide 0.1 % for 10 minute.  sodium hypochlorite 20 % and add Tween-20 (1%) shake for 10 min.  Wash the pieces several times with sterile water  In some cases should be change sodium hypochlorite concentration and time  If the explants is not clean should be use 0.1% solution of mercuric chloride for 2-5 min.
  • 9. Medium used  As a basal culture medium Anderson’s Rhododendron medium - AN (Anderson,1980) is efficiently used for shoot initiation  Alternatively for shoot induction and multiplication modified WPM (McCown Woody Plant Medium) (Lloyd and McCown,1980)  20 g/L sucrose, 6 g/L agar
  • 10. Hormones  Cytokinin group hormone commonly zeatin riboside apply to Initiation and multiplication shoots in blueberry  Zeatin 1.0 mg/L show high number shoot multiplication.  2ip-isopen-tenyladenine 2.0 mg/l, is the alternative hormone for shoot multiplication  TDZ- Thidiazuron, 1.0 mg/L is second alternative cytokinin for shoot multiplication.  IBA- Indole-3-butyric acid 0.1- 1.0 mg/L, is auxins group supported callus and root formation  GA3- Gibberellic acid 0.1-0.5 mg/L, have supported plant length
  • 11.
  • 12.
  • 13.
  • 14. pH for the blueberry media  In highbush blueberry micropropagation, shoot growth or plantlet development is also highly sensitive to other environmental conditions, including pH, temperature, sucrose, humidity and growing substrate  pH is adjusted 5.1-5.5 for shoot multiplication  Root formation and shoot thickness pH is 4.5-5.0.
  • 15. Root formation The best media for rooting :  Anderson medium or WPM supplemented with 0.8-1.0 mg/L IBA and 1.0 g/L activated charcoal and the pH adjusted 4.5  Sucrose 15 mg/L  Agar 6.5-7.0 g/L
  • 16. Acclimatization process  Primary hardening in mist chamber culture plants on peat substrate with green leaves and roots were first kept in the mist chamber for 14 days.  Graded plant were transferred nursery and spray NPK 19:19:19 5g/15 litter water with fungicide and regular irrigation and gradually lowering the humidity by ventilation for 2-4 weeks  Secondary hardening plantlets in height 8-10 cm (after 2 months) were replanted into bigger containers (12.0 cm in diameter) and transferred to open- air conditions.